Genetic Predisposition
Based on your genetic markers, your predisposition to this trait is shown below
Your Result
Lower Bulimia nervosa susceptibility predisposition
Was this result accurate for you?
Scientific Evidence
Understanding the Data
- SNP: A specific genetic marker relevant to this trait (e.g., rs2588978)
- Genotype: Your genetic makeup at the given SNP location (e.g., CC)
- Variant allele: The alternative DNA sequence at the SNP site
- Variant allele frequency: Percentage of population carrying this variant
- Variant found: Whether the variant was detected in your DNA file
AFF1 GeneCards
AF4/FMR2 family member 1
Genomic Location
No SNPs found for this gene in your DNA data.
C4orf36 GeneCards
Genomic Location
No SNPs found for this gene in your DNA data.
CCDC69 GeneCards
Genomic Location
No SNPs found for this gene in your DNA data.
CDV3 GeneCards
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs11708304 | -- | C | T | 85.30% | No Data |
CHODL GeneCards
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs77600076 | -- | A | C | 97.10% | No Data |
DAB1 GeneCards
The laminar organization of multiple neuronal types in the cerebral cortex is required for normal cognitive function. In mice, the disabled-1 gene plays a central role in brain development, directing the migration of cortical neurons past previously formed neurons to reach their proper layer. This gene is similar to disabled-1, and the protein encoded by this gene is thought to be a signal transducer that interacts with protein kinase pathways to regulate neuronal positioning in the developing brain. COMPLETENESS: complete on the 3' end.
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs985795 | -- | T | G | 94.60% | No Data |
GM2A GeneCards
This gene encodes a small glycolipid transport protein which acts as a substrate specific co-factor for the lysosomal enzyme beta-hexosaminidase A. Beta-hexosaminidase A, together with GM2 ganglioside activator, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene result in GM2-gangliosidosis type AB or the AB variant of Tay-Sachs disease. Alternative splicing results in multiple transcript variants.
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs7724774 | -- | G | A | 88.40% | No Data |
HSD17B11 GeneCards
Genomic Location
No SNPs found for this gene in your DNA data.
HSD17B13 GeneCards
hydroxysteroid 17-beta dehydrogenase 13
Genomic Location
No SNPs found for this gene in your DNA data.
KLHL8 GeneCards
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs115694618 | -- | A | G | 97.90% | No Data |
MAGI3 GeneCards
membrane associated guanylate kinase, WW and PDZ domain containing 3
Genomic Location
No SNPs found for this gene in your DNA data.
NKAIN3 GeneCards
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs142014203 | -- | T | G | 97.40% | No Data |
OLIG2 GeneCards
This gene encodes a basic helix-loop-helix transcription factor which is expressed in oligodendroglial tumors of the brain. The protein is an essential regulator of ventral neuroectodermal progenitor cell fate. The gene is involved in a chromosomal translocation t(14
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs117124364 | -- | C | T | 97.70% | No Data |
PCBD2 GeneCards
Genomic Location
No SNPs found for this gene in your DNA data.
PHTF1 GeneCards
putative homeodomain transcription factor 1
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs61742849 | -- | G | A | 97.50% | No Data |
PITX1 GeneCards
This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. Members of this family are involved in organ development and left-right asymmetry. This protein acts as a transcriptional regulator involved in basal and hormone-regulated activity of prolactin.
Genomic Location
No SNPs found for this gene in your DNA data.
PRM1 GeneCards
Genomic Location
No SNPs found for this gene in your DNA data.
PRM2 GeneCards
protamine 2
Genomic Location
No SNPs found for this gene in your DNA data.
PRM3 GeneCards
Genomic Location
No SNPs found for this gene in your DNA data.
SMTN GeneCards
This gene encodes a structural protein that is found exclusively in contractile smooth muscle cells. It associates with stress fibers and constitutes part of the cytoskeleton. This gene is localized to chromosome 22q12.3, distal to the TUPLE1 locus and outside the DiGeorge syndrome deletion. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms.
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs111383589 | -- | C | T | 89.20% | No Data |
SOCS1 GeneCards
suppressor of cytokine signaling 1
Genomic Location
No SNPs found for this gene in your DNA data.
TMPRSS15 GeneCards
This gene encodes an enzyme that converts the pancreatic proenzyme trypsinogen to trypsin, which activates other proenzymes including chymotrypsinogen and procarboxypeptidases. The precursor protein is cleaved into two chains that form a heterodimer linked by a disulfide bond. This protein is a member of the trypsin family of peptidases. Mutations in this gene cause enterokinase deficiency, a malabsorption disorder characterized by diarrhea and failure to thrive.
Genomic Location
No SNPs found for this gene in your DNA data.
TNP2 GeneCards
transition protein 2
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs117096873 | -- | C | T | 97.40% | No Data |
VSTM2B GeneCards
V-set and transmembrane domain containing 2B
Genomic Location
Associated SNPs
| SNP | Genotype | Ref. Allele | Variant Allele | Frequency | Status |
|---|---|---|---|---|---|
| rs12986207 | -- | G | A | 81.70% | No Data |
These are the genetic markers (SNPs) analyzed for this trait. Variations detected in your genome are listed under the "Genotype" column. SNPs showing "--" were not identified in your DNA file.
| SNP | Chromosome | Genotype | Variant Allele | Frequency |
|---|---|---|---|---|
| rs1556640 | TT | T | 88.00% | |
| rs145379083 | 4 | AA | A | 51.00% |
| rs61742849 | 1 | -- | A | 97.50% |
| rs985795 | 1 | -- | G | 94.60% |
| rs1445130 | 2 | -- | G | 86.40% |
| rs56148675 | 2 | -- | C | 94.20% |
| rs78661745 | 3 | -- | T | 90.80% |
| rs11708304 | 3 | -- | T | 85.30% |
| rs74879986 | 4 | -- | A | 97.50% |
| rs115694618 | 4 | -- | G | 97.90% |
| rs7724774 | 5 | -- | A | 88.40% |
| rs299362 | 5 | -- | A | 88.60% |
| rs2910124 | 5 | -- | T | 85.80% |
| rs28631020 | 6 | -- | A | 92.50% |
| rs142014203 | 8 | -- | G | 97.40% |
| rs6999631 | 8 | -- | C | 96.50% |
| rs8024343 | 15 | -- | T | 83.10% |
| rs8040855 | 15 | -- | C | 63.40% |
| rs117096873 | 16 | -- | T | 97.40% |
| rs12986207 | 19 | -- | A | 81.70% |
| rs77600076 | 21 | -- | C | 97.10% |
| rs117124364 | 21 | -- | T | 97.70% |
| rs111383589 | 22 | -- | T | 89.20% |
The following peer-reviewed scientific studies support the genetic associations analyzed in this report.
What's Next?
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